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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Arthrogryposis multiplex congenita
Arthrogryposis multiplex congenita 7, X-linked
rare
Identifiers
MONDO:0975826
OMIM:301127
Causal genes
THOC2
Part of
Arthrogryposis multiplex congenita
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